A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520177



Internal ID15447470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102456674..102474888hg38UCSC Ensembl
Innerchr9:105218956..105237170hg19UCSC Ensembl
Innerchr9:104258777..104276991hg18UCSC Ensembl
Innerchr9:102298511..102316725hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3818215
hg1918215
hg1818215
hg1718215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697265
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520177
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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